192126-19-5

Upstream product

• 192126-27-5 {(E)-3-Benzyloxymethyl-4-[1-methoxy-meth-(Z)-ylidene]-oct-5-enyloxy}-tert-butyl-dimethyl-silane 
• 192126-26-4 (Z)-2-[1-Benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-propyl]-hex-2-enal 
• 192126-28-6 (E)-3-Benzyloxymethyl-4-[1-methoxy-meth-(Z)-ylidene]-oct-5-en-1-ol 
• 192126-29-7 {(E)-2-(2-Iodo-ethyl)-3-[1-methoxy-meth-(Z)-ylidene]-hept-4-enyloxymethyl}-benzene 
• 192126-24-2 3-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-pentanal 
• 192126-23-1 (3-Benzyloxymethyl-hex-5-enyloxy)-tert-butyl-dimethyl-silane 
• 192126-22-0 2-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-pent-4-en-1-ol 
• 192126-21-9 2-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-pent-4-enal 
• 192126-33-3 (E)-5-Benzyloxymethyl-2-((E)-but-1-enyl)-6-[1-methoxy-meth-(Z)-ylidene]-2-trimethylsilanyloxy-dec-7-enenitrile 
• 192126-25-3 [3-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-pent-(E)-ylidene]-cyclohexyl-amine 

Relevant academic research and scientific papers

Synthesis of the bicyclic core of CP-225,917 and CP-263,114 by an intramolecular Diels-Alder reaction

New lead compounds with promising biological activity are represented by CP-225,917 and CP-263,114. An approach based on an intramolecular Diels Alder reaction for the total synthesis of these compounds is exemplified by the synthesis of racemic bicyclo[4.3.1]dec-1(9),4-dienes 2 a.b from triene 1.